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Important: This site presents data from the FDA Adverse Event Reporting System (FAERS). A report does not mean the drug caused the event. Full disclaimer.

Does ASCORBIC ACID\CRANBERRY Cause Product use in unapproved indication? 9 Reports in FDA Database

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According to the FDA Adverse Event Reporting System (FAERS), 9 reports of Product use in unapproved indication have been filed in association with ASCORBIC ACID\CRANBERRY. This represents 37.5% of all adverse event reports for ASCORBIC ACID\CRANBERRY.

9
Reports of Product use in unapproved indication with ASCORBIC ACID\CRANBERRY
37.5%
of all ASCORBIC ACID\CRANBERRY reports
0
Deaths
8
Hospitalizations

How Dangerous Is Product use in unapproved indication From ASCORBIC ACID\CRANBERRY?

Of the 9 reports, 8 (88.9%) required hospitalization, and 8 (88.9%) were considered life-threatening.

Is Product use in unapproved indication Listed in the Official Label?

This adverse event is not currently listed in the official FDA drug label for ASCORBIC ACID\CRANBERRY. However, 9 reports have been filed with the FAERS database.

What Other Side Effects Does ASCORBIC ACID\CRANBERRY Cause?

Balance disorder (17) Fall (17) Cognitive disorder (16) Hypotension (16) Orthostatic hypotension (16) Constipation (15) Sedation (15) Blood calcium decreased (14) Creatinine renal clearance decreased (14) Depressed level of consciousness (13)

What Other Drugs Cause Product use in unapproved indication?

DUPILUMAB (33,452) DICLOFENAC (12,197) METHOTREXATE (8,930) PREDNISONE (7,625) RITUXIMAB (7,519) MYCOPHENOLATE MOFETIL (5,910) ACETAMINOPHEN (5,819) CYCLOPHOSPHAMIDE (5,750) RISPERIDONE (5,551) TACROLIMUS (5,057)

Related Pages

ASCORBIC ACID\CRANBERRY Full Profile All Product use in unapproved indication Reports All Drugs Causing Product use in unapproved indication ASCORBIC ACID\CRANBERRY Demographics